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1 Ergebnisse
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Integration of whole genome sequencing into a healthcare se..:
Henrik Stranneheim
;
Kristina Lagerstedt-Robinson
;
Måns Magnusson
...
https://doi.org/10.1186/s13073-021-00855-5. , 2021
Link:
https://doi.org/10.1186/s13073-021-00855-5
RT Journal T1
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:24239a4e507a406db912b81371637d5d&Exemplar=1&LAN=DE A1 Henrik Stranneheim A1 Kristina Lagerstedt-Robinson A1 Måns Magnusson A1 Malin Kvarnung A1 Daniel Nilsson A1 Nicole Lesko A1 Martin Engvall A1 Britt-Marie Anderlid A1 Henrik Arnell A1 Carolina Backman Johansson A1 Michela Barbaro A1 Erik Björck A1 Helene Bruhn A1 Jesper Eisfeldt A1 Christoph Freyer A1 Giedre Grigelioniene A1 Peter Gustavsson A1 Anna Hammarsjö A1 Maritta Hellström-Pigg A1 Erik Iwarsson A1 Anders Jemt A1 Mikael Laaksonen A1 Sara Lind Enoksson A1 Helena Malmgren A1 Karin Naess A1 Magnus Nordenskjöld A1 Mikael Oscarson A1 Maria Pettersson A1 Chiara Rasi A1 Adam Rosenbaum A1 Ellika Sahlin A1 Eliane Sardh A1 Tommy Stödberg A1 Bianca Tesi A1 Emma Tham A1 Håkan Thonberg A1 Virpi Töhönen A1 Ulrika von Döbeln A1 Daphne Vassiliou A1 Sofie Vonlanthen A1 Ann-Charlotte Wikström A1 Josephine Wincent A1 Ola Winqvist A1 Anna Wredenberg A1 Sofia Ygberg A1 Rolf H. Zetterström A1 Per Marits A1 Maria Johansson Soller A1 Ann Nordgren A1 Valtteri Wirta A1 Anna Lindstrand A1 Anna Wedell PB BMC YR 2021 K1 Whole genome sequencing K1 Monogenic disease K1 Single nucleotide variant K1 Clinical diagnostics K1 Medicine K1 R K1 Genetics K1 QH426-470 JF https://doi.org/10.1186/s13073-021-00855-5 LK http://dx.doi.org/https://doi.org/10.1186/s13073-021-00855-5 DO https://doi.org/10.1186/s13073-021-00855-5 SF ELIB - SuUB Bremen
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